Canonical Allele Identifier: CA379092353

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1774759C>G (hg19) ; chr11:g.1753529C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753529C>G , CM000673.2:g.1753529C>G	GRCh38
NC_000011.9:g.1774759C>G , CM000673.1:g.1774759C>G	GRCh37
NC_000011.8:g.1731335C>G	NCBI36
NG_008655.1:g.15464G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1213G>C MANE Select	ENSP00000236671.2:p.Gly405Arg
ENST00000367196.4:c.1108G>C	ENSP00000356164.4:p.Gly370Arg
ENST00000427721.3:c.634+4G>C
ENST00000429746.2:c.1108G>C	ENSP00000402586.2:p.Gly370Arg
ENST00000433655.6:c.*379G>C	ENSP00000404902.1:n.*379G>C
ENST00000438213.6:c.1330G>C	ENSP00000415036.2:p.Gly444Arg
ENST00000636397.1:c.1071+274G>C	ENSP00000489910.1:n.1071+274G>C
ENST00000636571.1:c.1192G>C	ENSP00000490770.1:p.Gly398Arg
ENST00000636579.1:c.72+274G>C	ENSP00000490489.1:n.72+274G>C
ENST00000636615.1:c.1071+274G>C	ENSP00000490014.1:n.1071+274G>C
ENST00000636843.1:c.1207G>C	ENSP00000490897.1:p.Gly403Arg
ENST00000637158.1:n.811G>C
ENST00000637381.2:n.3641G>C
ENST00000637387.1:c.1192G>C	ENSP00000490598.1:p.Gly398Arg
ENST00000637815.2:c.1195G>C	ENSP00000490344.1:p.Gly399Arg
ENST00000637915.1:c.1204G>C	ENSP00000490471.1:p.Gly402Arg
ENST00000637937.1:n.521G>C
ENST00000678991.1:c.*1074G>C	ENSP00000503019.1:n.*1074G>C
ENST00000236671.6:c.1213G>C	ENSP00000236671.2:p.Gly405Arg
ENST00000427721.2:c.471+274G>C	ENSP00000415840.2:n.471+274G>C
ENST00000429746.1:c.544G>C	ENSP00000402586.1:p.Gly182Arg
ENST00000433655.5:c.*379G>C	ENSP00000404902.1:n.*379G>C
NM_001909.4:c.1213G>C	NP_001900.1:p.Gly405Arg
NM_001909.5:c.1213G>C MANE Select	NP_001900.1:p.Gly405Arg